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Power-Trialysis 5607200B

by Bard Access Systems, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00801741238260 UDI-DI Date13 Apr 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Power-Trialysis
Generic Name
Triple-lumen haemodialysis catheter
Model / Ref / Catalog
5607200B
Primary DI / UDI-DI
00801741238260
FDA Product Code
NIE
GMDN Term
Triple-lumen haemodialysis catheter
Device Class
Class II
Regulation Number
876.5540
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe
Size
Catheter Gauge — 13 French
Length — 20 Centimeter

Other devices from Bard Access Systems, Inc.

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No